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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7084172copy number variation1nstd229human GRCh38 chrX: 135,358,481-135,359,427 , GRCh37.p13 chrX|NW_004070887.1: 289,624-290,570 , GRCh37.p13 chrX: 134,492,406-134,493,352 ZNF449
    nsv7084171copy number variation1nstd229human GRCh38 chrX: 135,345,017-135,480,190 , GRCh37.p13 chrX|NW_004070887.1: 276,160-411,333 , GRCh37.p13 chrX: 134,478,942-134,614,115 ZNF449, WDR4P1, 5 more genes
    nsv7084158copy number variation1nstd229human GRCh38 chrX: 135,162,941-135,360,684 , GRCh37.p13 chrX|NW_004070887.1: 94,085-291,827 , GRCh37.p13 chrX: 134,296,866-134,494,609 LOC650024, ETDC, 8 more genes
    nsv7055541inversion1nstd229human GRCh38 chrX: 135,171,829-135,507,073 , GRCh37.p13 chrX|NW_004070887.1: 102,973-438,216 , GRCh37.p13 chrX: 134,305,753-134,640,998 LOC105373342, CROCCP1, 13 more genes
    nsv7054807inversion1nstd229human GRCh38 chrX: 135,168,027-135,425,482 , GRCh37.p13 chrX|NW_004070887.1: 99,171-356,625 , GRCh37.p13 chrX: 134,301,951-134,559,407 ETDC, LOC650024, 10 more genes
    nsv7053317inversion1nstd229human GRCh38 chrX: 135,179,664-135,609,734 , GRCh37.p13 chrX: 134,313,588-134,743,659 , GRCh37.p13 chrX|NW_004070887.1: 110,808-540,877 WDR4P1, LOC100421043, 16 more genes
    nsv7044060inversion1nstd229human GRCh38 chrX: 134,736,748-136,484,102 , GRCh37.p13 chrX|NW_004070887.1: 1-1,045,622 , GRCh37.p13 chrX: 133,870,778-135,566,261 ETDA, SAGE3P, 57 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634205copy number variation1nstd224human GRCh37 chrX: 134,390,692-134,852,104 , GRCh38.p12 chrX: 135,256,744-135,718,343 ZNF75D, INTS6L, 16 more genes
    nsv6634204copy number variation1nstd224human GRCh37 chrX: 134,292,131-134,841,419 , GRCh38.p12 chrX: 135,158,206-135,707,704 ZNF75D, INTS6L, 20 more genes
    nsv6633826copy number variation1nstd224human GRCh37 chrX: 134,292,131-134,786,450 , GRCh38.p12 chrX: 135,158,206-135,652,735 ZNF75D, INTS6L, 18 more genes
    nsv6633825copy number variation1nstd224human GRCh37 chrX: 134,292,131-134,537,928 , GRCh38.p12 chrX: 135,158,206-135,404,003 LOC650024, ETDA, 9 more genes
    nsv6633775copy number variation1nstd224human GRCh37 chrX: 133,906,202-135,831,362 , GRCh38.p12 chrX: 134,772,172-136,749,203 GAPDHP67, VGLL1, 63 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
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